Abstract

Degradation of residual lignin in kraft pulp by chemical bleaching is implicated in causing environmental pollution. The use of thermo- and alkali-tolerant bacterial laccases is considered to be important biological alternative to chemical processing. Laccases from Bacillus species have shown promise in this respect but their intracellular/spore bound presence make their industrial application economically unfeasible. We report here on a novel extracellular active thermo-alkali-stable laccase (SN4 laccase) which is active at 90 °C and pH 8.0 using 2,6-dimethoxyphenol as substrate from Bacillus tequilensis SN4. SN4 laccase retained 27 % activity for 5 min at 100 °C and more than 80 % activity for 24 h at 70 °C. The enzyme is also stable at a higher pH (9.0–10.0). Enzyme production was optimized by submerged fermentation. Relatively high yields (18,356 nkats ml−1) of SN4 laccase was obtained in a medium containing 650 μM MnSO4, 350 μM FeSO4, and 3.5 % ethanol. A 764-fold increase in laccase activity was observed under optimal conditions. In addition, reduction in kappa number and increase in brightness of softwood pulp by 28 and 7.6 %, respectively, were observed after treatment with SN4 laccase without a mediator. When N-hydroxybenzotriazole was used as a mediator, the kappa number was decreased to 47 % and brightness was increased to 12 %.

Highlights

  • Laccases are multicopper oxidases, which catalyze the oxidation of a wide variety of organic and inorganic compounds with concomitant four-electron reduction of molecular oxygen to water

  • We report here on a novel extracellular active thermo-alkali-stable laccase (SN4 laccase) which is active at 90 °C and pH 8.0 using 2,6dimethoxyphenol as substrate from Bacillus tequilensis SN4

  • B. tequilensis SN4 was isolated from the activated sludge of paper mill effluent treatment plant, which was found to produce an extracellular laccase

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Summary

Introduction

Laccases (benzenediol:oxygen oxidoreductases; EC 1.10.3.2) are multicopper oxidases, which catalyze the oxidation of a wide variety of organic and inorganic compounds with concomitant four-electron reduction of molecular oxygen to water. They catalyze the oxidation of both phenolic and non-phenolic substrates (Imran et al 2012). They were first observed in the exudates of Japanese lacquer tree Rhus vernicifera (Yoshida 1883) and have been found in almost all spheres of life but have been most extensively studied in fungi including Ascomycetes, Basidiomycetes, and Deuteromycetes (Brijwani et al 2010)

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